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H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs

GSE205249 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 156 samples Submitted 2026/03/02 Platform GPL21273Platform GPL24247Platform GPL24676Platform GPL16791Platform GPL20301Platform GPL20795
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 156 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Homo sapiens (human)
Samples
156 samples: 129 distinct titles, 26 of them repeatedGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programsNature genetics · 2026
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs
Krug B, Hu B, Chen H et al. · Nature genetics 2026 · PMID 42151415 · doi:10.1038/s41588-026-02586-y
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE205249_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA844270 and SRA study SRP377943. Searching any of these in the dataset finder brings you back here.

Study design
129 distinct titles, 26 of them repeated
HSJ019, K27M-KO, ×3 hiPSC, WT, H3K36me ×2 mESC, NSD1KO, CBX2, ×2 mESC, NSD1KO, RING1B, ×2 mESC, NSD1KO, inputForCBX2, ×2 mESC, NSD1KO, inputForRING1B, ×2 mESC, WT, CBX2, ×2 mESC, WT, RING1B, ×2 +18 more

How we read this: Read from 156 sample titles: 129 distinct titles with little repetition. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study

+ 116 more — browse all 156 samples with per-sample file links →

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.